What is another word for Glucosephosphatase Deficiency?
Pronunciation: [ɡlˈuːkə͡ʊsfˌɒsfɐtˌe͡ɪs dɪfˈɪʃənsi] (IPA) 
Glucosephosphatase Deficiency, also known as Glycogen Storage Disease type 1 (GSD1), is a rare genetic disorder that affects the body's ability to break down glycogen into glucose. Individuals with this condition often experience symptoms such as hypoglycemia, enlarged liver, growth delays, and muscle weakness. Though commonly referred to as Glucosephosphatase Deficiency, it is important to note that this condition has alternative names, including Von Gierke disease, Hepatorenal Glycogenosis, and GSD type Ia. All these terms indicate the same disorder but may be used interchangeably by medical professionals and researchers when discussing the condition.
